Switzerland’s drug regulator, Swissmedic, has streamlined its procedure for companies seeking a fast-track evaluation or a temporary authorization of their products by dispensing with the need for them to take part in accelerated application hearings (AAAs) in certain cases.
Swiss Agency Optimizes Fast-Track Review, Temporary Authorization Routes
Swissmedic has removed the requirement for companies to participate in accelerated application hearings in certain situations.

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The European Medicines Agency has recommended five drugs for EU-wide approval , including Averoa’s Xoanacyl for concomitant hyperphosphatemia. Two companies have withdrawn their marketing authorization applications.
Eli Lilly’ will request a re-examination after the European Medicines Agency declined to recommend its Alzheimer’s disease drug Kisunla for EU approval.